57861294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88085334-C-T

57861357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88085274-T-C

57861423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88085169-T-C

57861433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88085159-G-A

57861433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88085159-G-T

57861443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88085126-G-A

57861445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88085124-G-A

57861450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88085110-G-A

57861450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88085110-G-T

57861457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88085103-A-G

57861462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88085098-C-G

57861462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88085098-C-T

57861577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88084977-G-A

57861577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88084977-G-T

http://identifiers.org/hco/17/GRCh38#57861761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88084791-C-A

http://identifiers.org/hco/17/GRCh38#57862154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88084453-C-A

57862154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88084453-C-T

57862219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88084388-G-T

57862266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88084358-G-A

57862266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88084358-G-T

http://identifiers.org/hco/17/GRCh38#57862293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88084336-C-A

57862367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88084256-T-C

57862372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88084251-C-G

57862372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88084251-C-T

57862557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88084073-G-A

57862557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88084073-G-T

http://identifiers.org/hco/17/GRCh38#57862582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88084046-C-A

57862582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88084046-C-T

57862622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88084002-G-C

57862622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88084002-G-T

http://identifiers.org/hco/17/GRCh38#57862763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88083928-A-C

57862763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88083928-A-G

57862770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88083921-G-T

57862775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88083916-G-A

57862786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88083905-C-T

57862788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88083903-G-A

57862788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88083903-G-T

57862790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88083901-A-G

http://identifiers.org/hco/17/GRCh38#57862906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88083812-C-A

57862906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88083812-C-T

57862942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88083778-A-G

57862962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88083752-A-G

57862975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88083728-T-A

57862975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88083728-T-C

57863400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88083333-C-G

57863416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88083317-G-A

57863416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88083317-G-T

57863538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88083221-C-T

57863615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88083143-A-G

57863629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88083125-G-C

57865099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88082323-G-A

57865099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88082323-G-C

57865100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88082322-T-C

57865298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88082170-C-T

57865421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88082065-T-C

57865579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88081898-G-C

57865642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88081833-G-A

57866447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88080975-C-G

57866570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88080854-A-T

57866591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88080833-C-T

http://identifiers.org/hco/17/GRCh38#57866688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88080749-C-A

57866688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88080749-C-T

57866694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88080743-T-C

57866723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88080715-G-A

57866723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88080715-G-C

57866723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88080715-G-T

57866871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88080572-A-G

57866963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88080490-T-C

57866963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88080490-T-G

http://identifiers.org/hco/17/GRCh38#57867264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88079769-C-A

57867264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88079769-C-G

57867264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88079769-C-T

http://identifiers.org/hco/17/GRCh38#57867310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88079713-C-A

57867417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 88079605-T-C

57867447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88079575-G-A

57867447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88079575-G-T

http://identifiers.org/hco/17/GRCh38#57867551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88079472-A-C

57867551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88079472-A-G

57867553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88079470-T-G

57867604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88079415-A-G

http://identifiers.org/hco/17/GRCh38#57867609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88079410-C-A

http://identifiers.org/hco/17/GRCh38#57867653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88079365-C-A

57867653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88079365-C-T

57867679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88079339-T-G

http://identifiers.org/hco/17/GRCh38#57867685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88079333-C-A

57867685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88079333-C-T

57867752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88079252-G-A

http://identifiers.org/hco/17/GRCh38#57868085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88078974-C-A

57868085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88078974-C-G

57868085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88078974-C-T

57868293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88078765-G-C

57868293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88078765-G-T

57868328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88078729-A-G

57868330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88078727-G-T

57868336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88078717-G-A

57868336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88078717-G-C

57868336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88078717-G-T

http://identifiers.org/hco/17/GRCh38#57868550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88078524-C-A

57868550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88078524-C-T

57868574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88078500-G-A

57868574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88078500-G-T

http://identifiers.org/hco/17/GRCh38#57868578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88078489-C-A

57868578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88078489-C-T

57868632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88078436-G-A

57868789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88078272-C-T

57868834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88078239-C-T

57869105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88077973-G-A

57869105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88077973-G-T

57869180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88077898-G-C

57869283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88077736-A-T

57869290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88077729-G-T

http://identifiers.org/hco/17/GRCh38#57869303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88077716-C-A

57869303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88077716-C-G

57869466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88077578-A-G

http://identifiers.org/hco/17/GRCh38#57869516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88077516-C-A

http://identifiers.org/hco/17/GRCh38#57869587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88077445-C-A

http://identifiers.org/hco/17/GRCh38#57869796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88077312-C-A

57869796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88077312-C-T

http://identifiers.org/hco/17/GRCh38#57869861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88077276-C-A

57869861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88077276-C-T

http://identifiers.org/hco/17/GRCh38#57869932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88077205-C-A

57869932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88077205-C-T

http://identifiers.org/hco/17/GRCh38#57869995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88077154-C-A

57870128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88077020-G-C

http://identifiers.org/hco/17/GRCh38#57871165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88075660-C-A

57871165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88075660-C-T

http://identifiers.org/hco/17/GRCh38#57871172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88075653-C-A

57871200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88075625-C-T

57871268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88075559-C-T

57871329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88075498-G-A

57871463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88075379-G-A

57871463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88075379-G-T

57871482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88075360-A-T

http://identifiers.org/hco/17/GRCh38#57871486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88075356-C-A

57871486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88075356-C-T

57872514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88074393-G-T

http://identifiers.org/hco/17/GRCh38#57872566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88074341-C-A

57872566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88074341-C-T

http://identifiers.org/hco/17/GRCh38#57872578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88074330-C-A

57872581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88074327-A-G

http://identifiers.org/hco/17/GRCh38#57872597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88074308-C-A

57872597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88074308-C-T

57872627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88074279-T-C

57872793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88074125-T-C

57872800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88074118-G-A

http://identifiers.org/hco/17/GRCh38#57872941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88074000-C-A

57872941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88074000-C-T

57873181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88073759-C-T

57873216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88073736-C-T

57873217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88073735-G-A

http://identifiers.org/hco/17/GRCh38#57873485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88073546-C-A

57873731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88073291-G-A

57873731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88073291-G-C

57873731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88073291-G-T

57873738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88073285-G-A

57873738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88073285-G-T

57873769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88073254-G-A

57874079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88073010-A-G

57874250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88072850-C-T

57874314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88072791-G-T

http://identifiers.org/hco/17/GRCh38#57874797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88072122-C-A

57874849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88072069-G-A

http://identifiers.org/hco/17/GRCh38#57874855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88072063-C-A

57874946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88071975-T-G

57875342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88071699-C-T

57875478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88071574-A-G

57877900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88069740-A-G

57877989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88069652-C-T

57878017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88069623-C-T

http://identifiers.org/hco/17/GRCh38#57878026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88069614-A-C

57878199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88069499-T-C

57878214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88069495-A-G

57878393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88069342-A-G

http://identifiers.org/hco/17/GRCh38#57879043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88069037-C-A

57879050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88069030-C-T

57879315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88068768-C-T

57879485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88068350-G-A

57879485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88068350-G-T

http://identifiers.org/hco/17/GRCh38#57879522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88068309-C-A

http://identifiers.org/hco/17/GRCh38#57879523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88068308-C-A

57879523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88068308-C-T

57879554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88068277-C-T

57879583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88068250-T-C

57879583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88068250-T-G

57879603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 88068229-A-T

57879668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88068164-T-C

57879731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88068101-T-C

http://identifiers.org/hco/17/GRCh38#57879808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88068002-A-C

http://identifiers.org/hco/17/GRCh38#57879835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88067973-A-C

57879959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88067868-C-T

57880022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88067805-A-G

57880930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88064264-G-A

http://identifiers.org/hco/17/GRCh38#57881940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88063465-A-C

57881942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88063463-C-T

http://identifiers.org/hco/17/GRCh38#57882214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88063217-C-A

57882476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88062970-C-G

57882556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88062896-C-T

57883150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88062771-C-T

57883155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88062766-G-A

57883166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88062755-T-C

57883236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88062683-C-T

57885102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88061148-G-T

57885188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88061037-T-A

http://identifiers.org/hco/17/GRCh38#57885189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88061036-C-A

57885221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 88061006-G-A

57885221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 88061006-G-T

57885433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88060800-G-T

57885511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88060710-G-A

57885511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88060710-G-T

http://identifiers.org/hco/17/GRCh38#57885553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88060668-C-A

http://identifiers.org/hco/17/GRCh38#57885574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88060647-C-A

http://identifiers.org/hco/17/GRCh38#57885658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88060563-C-A

57885658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88060563-C-T

57885663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88060558-G-A

http://identifiers.org/hco/17/GRCh38#57885671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88060550-C-A

57885671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88060550-C-T

57885803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88060473-C-G

57885803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88060473-C-T

http://identifiers.org/hco/17/GRCh38#57885834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88060442-C-A

57885834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88060442-C-G

57885834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88060442-C-T

57885899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88060372-A-G

57885899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88060372-A-T

57887067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88059909-C-T

57887229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88059730-C-T

57887425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88058977-G-A

http://identifiers.org/hco/17/GRCh38#57887445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88058957-A-C

57887933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88058007-G-T

57888058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88057892-G-A

57888092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88057868-G-C

57888131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88057813-G-C

57888613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88057414-C-G

http://identifiers.org/hco/17/GRCh38#57888693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88057354-C-A

http://identifiers.org/hco/17/GRCh38#57888827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88057249-C-A

57889169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88057029-G-C

57889193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88056997-G-A

57889193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88056997-G-C

57889709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88056602-A-G

57889787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88056559-C-T

http://identifiers.org/hco/17/GRCh38#57889876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88056491-C-A

57890676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88055734-T-C

57890859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88055542-T-G

57891021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88055368-G-A

57891027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88055362-G-A

57891156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88055255-A-G

57891248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88055159-G-A

57891263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88055152-C-T

57892665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88053108-T-C

http://identifiers.org/hco/17/GRCh38#57892751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88053023-C-A

57892751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88053023-C-G

57893021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88052779-G-C

57893021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88052779-G-T

57893046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88052767-G-C

57893238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88052587-G-A

57893238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88052587-G-T

57893287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88052538-G-A

57894919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88051274-G-A

57895469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88050174-G-A

57895792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88049849-C-T

57895970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88049718-G-A

57896129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88049575-C-G

57896129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88049575-C-T

57896207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88049497-A-G

57896481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88049156-T-G

57896509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88049134-T-G

57896634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88049081-A-G

57896634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88049081-A-T

http://identifiers.org/hco/17/GRCh38#57896799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88048972-C-A

57896799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88048972-C-G

57896799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88048972-C-T

http://identifiers.org/hco/17/GRCh38#57896801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88048970-C-A

57896801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88048970-C-G

57896801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88048970-C-T

57897183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88048781-A-G

57897213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88048751-A-T

57898248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88048021-T-C

http://identifiers.org/hco/17/GRCh38#57898476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88047896-C-A

57898678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88047746-G-A

57898678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88047746-G-T

57898692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88047733-C-G

57898970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88047491-G-T

57899285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88047234-C-T

http://identifiers.org/hco/17/GRCh38#57899438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88047082-A-C

57899607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88046927-C-T

57899883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88046686-C-T

57899884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88046685-T-A

http://identifiers.org/hco/17/GRCh38#57899893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88046676-C-A

57899965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88046592-A-T

57900551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88046041-A-T

57900603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88045991-C-T

57900660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88045934-G-C

57900843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88045677-A-G

http://identifiers.org/hco/17/GRCh38#57901110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88045290-C-A

57901253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88045156-C-T

57901807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88044679-G-A

57901807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88044679-G-C

57901858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88044628-T-G

57902681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88043095-C-T

57902700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88043076-G-C

57902778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88043001-A-G

57902904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88042917-T-C

57903017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88042827-A-G

57903121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88042727-G-T

57903140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88042708-C-T

57903149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88042700-A-G

57903153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88042696-G-A

57903153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88042696-G-T

57903172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88042690-G-T

57903192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88042680-G-A

57903192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88042680-G-T

http://identifiers.org/hco/17/GRCh38#57903199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88042673-C-A

57903199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88042673-C-T

57903230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88042635-G-A

57903230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88042635-G-T

57903238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88042627-A-G

57903286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88042611-C-T

http://identifiers.org/hco/17/GRCh38#57903402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88042497-C-A

57903990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88042076-T-C

57904110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88041928-T-C

57904191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88041862-G-A

57904291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88041785-G-A

57904403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88041694-G-T

57904526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88040485-C-T

http://identifiers.org/hco/17/GRCh38#57904671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88040283-C-A

57904671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88040283-C-G

57904671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88040283-C-T

57904673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88040281-T-C

57904726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88040232-A-G

57904727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88040231-T-C

57904735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88040220-G-A

57905497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88039423-T-C

57905526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88039396-C-G

57905574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88039354-C-T

57906098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88038791-T-C

57906413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88038469-C-T

57906600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88038321-T-C

http://identifiers.org/hco/17/GRCh38#57906971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88037848-C-A

http://identifiers.org/hco/17/GRCh38#57906973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88037846-C-A

57906973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88037846-C-G

http://identifiers.org/hco/17/GRCh38#57906975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88037844-A-C

57906991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88037828-G-A

57906991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88037828-G-T

57907108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88037680-G-A

57907414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88037384-T-A

57907478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88037315-A-G

57907963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88036878-C-T

57908035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88036812-G-A

57909535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88035774-G-A

57909626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88035684-A-G

57909627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88035683-G-A

57909717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88035633-T-G

http://identifiers.org/hco/17/GRCh38#57909842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88035519-A-C

57912112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88033559-G-A

57912112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88033559-G-T

57912254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88033407-G-A

57912254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88033407-G-T

57912256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88033405-T-C

57912577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88033059-T-C

57912577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88033059-T-G

57914850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88031817-T-C

57915250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88031470-G-C

57915265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88031455-A-G

57915357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88031373-A-G

57915831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88030885-G-A

57915832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88030884-G-A

57915966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88030761-T-C

57916178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88030571-G-A

57916326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88030414-G-A

57916334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88030404-C-T

57916848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88029942-T-C

57917054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88029724-C-T

57917071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88029710-A-G

57917171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88029546-G-C

57917832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88028729-G-T

57917883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88028681-T-A

57918032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88028583-A-T

http://identifiers.org/hco/17/GRCh38#57918310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88028318-C-A

57918310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88028318-C-T

http://identifiers.org/hco/17/GRCh38#57918518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88028174-C-A

57918518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88028174-C-T

57918586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88028095-T-C

57919606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88026940-C-T

http://identifiers.org/hco/17/GRCh38#57920203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88026222-A-C

57920413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88026046-T-C

57920427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88026032-C-T

57920787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88025699-C-T

57920835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88025572-C-T

57921218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88024674-C-T

57921246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88024645-G-A

57921335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88024572-C-T

57921671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

57921821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

57921828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

57923177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88023148-A-G

57923887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88022334-A-G

57924139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88021999-C-G

57924139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88021999-C-T

http://identifiers.org/hco/17/GRCh38#57924504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88021522-A-C

57924956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88021119-T-C

57925633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88020441-T-C

57925763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88020326-G-A

57926157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88019933-A-G

57926321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88018271-C-T

57926390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88018136-C-T

57926464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88018053-G-A

57927224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88017251-G-A

57927560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88016950-C-T

57927646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88016882-A-G

57927668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88016860-C-T

57928141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88016163-C-G

57928141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88016163-C-T

57928152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88016149-A-T

57928162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88016137-A-T

57928439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88015815-C-T

57928539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88015724-T-A

57928539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88015724-T-C

57928696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88015307-C-T

57928738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88015264-A-G

57928821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88015181-G-A

http://identifiers.org/hco/17/GRCh38#57928959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88015029-A-C

57929167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88014976-A-G

57929296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88014871-T-C

57929309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88014858-A-G

57929564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88014720-A-G

57930255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88014181-C-T

57930287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88014161-G-C

57930381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88014062-T-A

57930428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88014015-G-A

57930428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88014015-G-T

57930429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88014014-C-T

57930522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88013922-G-T

57930592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88013868-T-A

57930655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88013815-C-T

57931381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88013001-T-C

57931573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88012843-G-C

57931685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88012730-C-T

57931709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88012691-C-T

57932100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88012345-C-T

57932128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88012314-A-G

57932189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88012260-C-G

57932280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88012133-T-A

57932280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88012133-T-C

http://identifiers.org/hco/17/GRCh38#57933365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88011725-C-A

57933387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88011704-T-C

57933398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88011693-G-C

57933483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88011608-C-G

57933766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88011319-A-T

http://identifiers.org/hco/17/GRCh38#57935406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88010491-A-C

http://identifiers.org/hco/17/GRCh38#57935571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88010323-C-A

57935879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88010003-C-T

57935941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88009937-T-C

57936097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88009764-C-G

57936671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88009057-T-G

57936732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88008990-C-G

57937064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88008796-C-T

http://identifiers.org/hco/17/GRCh38#57937168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88008695-A-C

57938143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88008428-C-T

57938463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88008123-C-T

57938466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88008120-T-C

57938466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88008120-T-G

57938513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88008073-G-A

http://identifiers.org/hco/17/GRCh38#57939647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88007902-A-C

http://identifiers.org/hco/17/GRCh38#57939789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88007756-A-C

57939877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88007670-T-A

57940274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88007336-T-A

57940274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88007336-T-C

57940274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88007336-T-G

http://identifiers.org/hco/17/GRCh38#57940392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88007220-C-A

57940563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88006569-T-C

http://identifiers.org/hco/17/GRCh38#57940858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88006258-C-A

57940969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88006146-C-T

http://identifiers.org/hco/17/GRCh38#57941119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88005962-A-C

57941119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88005962-A-G

57941221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88005857-C-G

57941221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88005857-C-T

57941237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88005841-C-T

57941271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88005807-C-G

57941271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88005807-C-T

57941503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88005574-C-T

57941856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88004834-T-C

57941907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88004784-C-T

57941967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88004724-C-T

57942181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88004539-G-A

http://identifiers.org/hco/17/GRCh38#57942347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88004376-A-C

57943268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88003187-G-A

57943287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88003169-G-A

57943320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88003136-C-T

57943566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88002945-G-A

57943699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88002815-G-A

57943775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88002741-G-C

http://identifiers.org/hco/17/GRCh38#57943859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88002670-A-C

http://identifiers.org/hco/17/GRCh38#57943934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88002596-C-A

57943934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88002596-C-T

57943962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88002582-A-G

57944726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88001149-T-C

57944832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88001034-C-T

57944900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88000967-A-G

57945341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88000542-C-T

57946493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87999674-T-C

57946704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87998704-G-A

57946759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87998645-T-C

57946881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87998532-G-C

57947125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87998294-T-A

57947125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87998294-T-C

57947438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87997662-T-G

57948382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87997154-G-A

57948383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87997153-G-A

57951198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87994228-G-C

57951673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87993475-G-A

57951702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87993427-A-G

57951881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87993287-T-C

http://identifiers.org/hco/17/GRCh38#57951887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#87993281-C-A

57951997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87993205-G-C

http://identifiers.org/hco/17/GRCh38#57952826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#87992392-C-A

57952965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87992263-C-T

57953041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87992191-T-G

57953131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87992095-A-G

57953182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87992052-G-A

57953182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87992052-G-T

http://identifiers.org/hco/17/GRCh38#57953765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#87991528-C-A

57954544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87990811-T-G

57954777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87990577-C-T

57954911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87990439-C-T

57954934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87990422-T-C

57954954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87990409-G-A

57954978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87990385-G-A

http://identifiers.org/hco/17/GRCh38#57955000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#87990363-A-C

57955257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87990136-G-A

57955257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87990136-G-C

57955257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87990136-G-T

57955265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87990128-G-A

57955307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87990095-G-T

http://identifiers.org/hco/17/GRCh38#57955332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#87990072-C-A

57955332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31350
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87990072-C-T